These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 15897646)

  • 1. A mother and a child with maternally inherited diabetes and deafness (MIDD) showing atrophy of the cerebrum, cerebellum and brainstem on magnetic resonance imaging (MRI).
    Kobayashi Z; Tsunemi T; Miake H; Tanaka S; Watabiki S; Morokuma Y
    Intern Med; 2005 Apr; 44(4):328-31. PubMed ID: 15897646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.
    Lien LM; Lee HC; Wang KL; Chiu JC; Chiu HC; Wei YH
    Acta Neurol Scand; 2001 Mar; 103(3):159-65. PubMed ID: 11240563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brain anomalies in maternally inherited diabetes and deafness syndrome.
    Fromont I; Nicoli F; Valéro R; Felician O; Lebail B; Lefur Y; Mancini J; Paquis-Flucklinger V; Cozzone PJ; Vialettes B
    J Neurol; 2009 Oct; 256(10):1696-704. PubMed ID: 19536585
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM; Lemkes HH; Gerbitz KD; Maassen JA
    Muscle Nerve Suppl; 1995; 3():S124-30. PubMed ID: 7603513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA; van den Ouweland JM; t Hart LM; Lemkes HH
    Horm Metab Res; 1997 Feb; 29(2):50-5. PubMed ID: 9105898
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chorea triggered by hyperglycemia in a maternally inherited diabetes and deafness (MIDD) patient with the A3243G mutation of mitochondrial DNA and basal ganglia calcification.
    Kang JH; Kang SY; Choi JC; Lee SS; Kim JS
    J Neurol; 2005 Jan; 252(1):103-5. PubMed ID: 15654564
    [No Abstract]   [Full Text] [Related]  

  • 8. Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.
    Schleiffer T; 't Hart LM; Schürfeld C; Kraatz K; Riemann JF
    Exp Clin Endocrinol Diabetes; 2000; 108(2):81-5. PubMed ID: 10826513
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L; Caruso RA; Zuccarello D; Rigoli M; Barberi I
    Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome.
    Jiang Z; Zhang Y; Yan J; Li F; Geng X; Lu H; Wei X; Feng Y; Wang C; Jia W
    J Diabetes Res; 2019; 2019():5184647. PubMed ID: 31143779
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.
    Bergamin CS; Rolim LC; Dib SA; Moisés RS
    Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1345-9. PubMed ID: 19169492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.
    Murphy R; Turnbull DM; Walker M; Hattersley AT
    Diabet Med; 2008 Apr; 25(4):383-99. PubMed ID: 18294221
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.
    Mory PB; Santos MC; Kater CE; Moisés RS
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):574-7. PubMed ID: 23295301
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.
    Oishi N; Kubota D; Nakamoto K; Takeda Y; Hayashi M; Gocho K; Yamaki K; Igarashi T; Takahashi H; Kameya S
    Ophthalmic Genet; 2021 Jun; 42(3):304-311. PubMed ID: 33541179
    [No Abstract]   [Full Text] [Related]  

  • 15. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C; Widjaja A; Boeck N; Skamira C; Zühlke H
    Exp Clin Endocrinol Diabetes; 1998; 106(5):384-8. PubMed ID: 9831303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.
    van Essen EH; Roep BO; 't Hart LM; Jansen JJ; Van den Ouweland JM; Lemkes HH; Maassen JA
    Diabet Med; 2000 Dec; 17(12):841-7. PubMed ID: 11168326
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA; Jansen JJ; van den Ouweland JM; Hart LM; van Essen EH; Lemkes HH
    Ned Tijdschr Geneeskd; 1998 Jan; 142(5):229-33. PubMed ID: 9557035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA.
    Tanaka K; Takada Y; Matsunaka T; Yuyama S; Fujino S; Maguchi M; Yamashita S; Yuba I
    Intern Med; 2000 Mar; 39(3):249-52. PubMed ID: 10772130
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
    Tabebi M; Charfi N; Kallabi F; Alila-Fersi O; Ben Mahmoud A; Tlili A; Keskes-Ammar L; Kamoun H; Abid M; Mnif M; Fakhfakh F
    J Diabetes Complications; 2017 Jan; 31(1):253-259. PubMed ID: 27422531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Establishment and application of quantitative detection for heteroplasmic mtDNA mutation 3243A→G].
    Zhang X; Chen L; Yang Y; Zheng C; Yan J; Lu Z; Lyu J; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):438-43. PubMed ID: 25119906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.